特发性炎症性肌炎中的低血清补体:临床特征及对预后的影响。

IF 2.7 Q3 IMMUNOLOGY
Shun Nomura, Yasuhiro Shimojima, Dai Kishida, Takanori Ichikawa, Akira Matsushima, Yoshiki Sekijima
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引用次数: 0

摘要

本研究探讨了特发性炎症性肌炎(IIM)患者血清补体水平下降的临床特征和预后相关性。研究比较了血清补体水平低于正常(L-Com)的特发性炎症性肌炎患者和血清补体水平正常(N-Com)的特发性炎症性肌炎患者的临床信息。在间质性肺病(ILD)患者中,采用回归分析法研究 L-Com 对其 PaO2/FiO2 (P/F) 比值的影响。使用对数秩检验评估了 ILD 的预后结果。在94例IIM患者中,26例患有L-Com(中位年龄为56.0岁),68例患有N-Com(56.5岁)。女性在 L-Com 患者中的比例(92.3%)明显高于 N-Com 患者(67.6%)。在 17 名 L-Com 患者(65.4%)和 46 名 N-Com 患者(67.6%)中观察到了 ILD。在患有 ILD 的患者中,L-Com 患者的 P/F 比值明显低于 N-Com 患者。血清 C3 水平与 P/F 比值下降相关。L-Com患者的ILD预后明显较差,尤其是在抗黑色素瘤分化相关蛋白5抗体阳性的患者中。L-Com可能与IIM相关ILD患者动脉血氧水平降低和预后较差有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low serum complements in idiopathic inflammatory myositis: clinical features and impact on the prognosis.

This study investigated the clinical features and prognostic relevance of decreased serum complement levels in patients with idiopathic inflammatory myositis (IIM). The clinical information of IIM patients with less than normal serum complement levels (L-Com) and that of those with normal serum complement levels (N-Com) was compared. In patients with interstitial lung disease (ILD), regression analyses were used to investigate the implication of L-Com in their PaO2/FiO2 (P/F) ratio. Prognostic outcomes of ILD were evaluated using the log-rank test. Of 94 IIM patients, 26 with L-Com (median age, 56.0 years) and 68 with N-Com (56.5 years) were included. The prevalence of women was significantly higher in patients with L-Com (92.3%) than in those with N-Com (67.6%). ILD was observed in 17 (65.4%) patients with L-Com and in 46 (67.6%) with N-Com. Among patients with ILD, the P/F ratio was significantly lower in those with L-Com than in those with N-Com. Serum C3 levels were correlated with decreased P/F ratio. Inferior prognosis of ILD was significantly demonstrated in patients with L-Com, especially in those positive for anti-melanoma differentiation-associated protein 5 antibody. L-Com may be implicated in reduced arterial oxygen levels and a poorer prognosis in patients with IIM-related ILD.

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来源期刊
Immunological Medicine
Immunological Medicine Medicine-Immunology and Allergy
CiteScore
7.10
自引率
2.30%
发文量
19
审稿时长
19 weeks
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